FDA UDI In Commercial Distribution 🇺🇸 United States

SonoTAP® II

DI: 04048223127865 · Model: 1285-3F150 · Pajunk GmbH Medizintechnologie
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
SonoTAP® II
Primary DI
04048223127865
Version / Model
1285-3F150
Catalog Number
1285-3F150
Company Name
Pajunk GmbH Medizintechnologie
Labeler DUNS
317654283
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-17
Public Version
3
Public Version Date
2025-06-30
Public Version Status
Update
Public Device Record Key
ce193fe6-9ad6-482e-bf9f-1c1590b2f9f2

Device Description

SonoTAP® II 21G x 150mm wit bevel tip and Cornerstone Reflectors

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

GMDN Terms

Code Name
61547 Peripheral nerve-block sharp needle

Identifiers

Type ID
Package 04048223129753
Primary 04048223127865
Previous 04048223116296

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K113207 000
K243525 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
20 – 65 Percent (%) Relative Humidity